4.7 Article

First insight into how stress exposure triggers Vibrio harveyi recipient successful conjugation

Journal

FRONTIERS IN MARINE SCIENCE
Volume 10, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmars.2023.1083714

Keywords

Vibrio harveyi; stress exposure; horizontal gene transfer; induced fertility; environmental regulation

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This study systematically analyzed the effect of environmental stress on the conjugation ability of the marine fish pathogen Vibrio harveyi. The results showed that certain stress exposure can induce the fertility of V. harveyi and promote the transfer of shuttle plasmids from Escherichia coli. Ethanol and heat stress exhibited the strongest induction effect. These findings will contribute to the development of gene knockout technology and advance the molecular theoretical research on V. harveyi, as well as support the establishment of disease prevention and control strategies based on environmental regulation of gene transfer.
Conjugation is the most common horizontal gene transfer (HGT) process that can be affected by environmental change and promote bacterial virulence and drug resistance. However, it is unknown whether environmental changes can influence the conjugation ability of the marine fish pathogen Vibrio harveyi, thereby affecting its pathogenicity and drug resistance. This study systematically analyzes the effect of environmental stress on the ability of V. harveyi to obtain shuttle plasmids from Escherichia coli during conjugation. The results indicate that V. harveyi cannot receive shuttle plasmid pMMB207 without exposure to stress. However, certain stress exposure (37-46 degrees C, 4%-16% ethanol, 0.14-0.56 mM SDS, 0.04 similar to 0.05 M NaOH, and 0.012-0.024 M HCl for 5-60 minutes) in the log phase of V. harveyi before conjugation successfully induces the fertility of the V. harveyi recipient in intergeneric mating with E. coli. In particular, ethanol and heat stress showed strong induction with up to 2.5 x 10(5) and 5.3 x 10(3) transconjugants when exposed to 16% ethanol for 10 minutes and 40 degrees C for 60 minutes, respectively. Additionally, appropriate levels of NaOH (0.05 M, 10 minutes), SDS (0.42 mM, 5 minutes), and HCl (0.024 M, 5 minutes) lead to 2.3 x 10(3), 4.5x10(2), and 1.8 x 10(2) transconjugants, respectively. These results will help establish homologous recombination gene knockout technology and greatly advance molecular theoretical research on V. harveyi. They will also support the establishment of disease prevention and control strategies based on the interruption of the HGT process by environmental regulation.

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